Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HA88
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.567 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.211 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.619 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.596 |
DOC_CYCLIN_RxL_1 | 244 | 254 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 105 | 117 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 392 | 400 | PF00069 | 0.372 |
DOC_MAPK_HePTP_8 | 390 | 402 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 393 | 402 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.368 |
DOC_PP1_RVXF_1 | 391 | 398 | PF00149 | 0.384 |
DOC_PP4_FxxP_1 | 544 | 547 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.209 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.310 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 549 | 553 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 555 | 560 | PF00244 | 0.367 |
LIG_BIR_III_4 | 470 | 474 | PF00653 | 0.383 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.311 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.398 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.359 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.352 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.397 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.571 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.490 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.497 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.417 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 543 | 547 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 216 | 223 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 445 | 452 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 540 | 548 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 97 | 103 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.196 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.275 |
LIG_NRBOX | 150 | 156 | PF00104 | 0.337 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.405 |
LIG_RPA_C_Fungi | 586 | 598 | PF08784 | 0.442 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.205 |
LIG_SH2_GRB2like | 327 | 330 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 98 | 102 | PF00017 | 0.303 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.451 |
LIG_SH2_SRC | 327 | 330 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 357 | 360 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.682 |
LIG_SUMO_SIM_anti_2 | 77 | 83 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 413 | 420 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.581 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.486 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.555 |
LIG_TRAF2_1 | 551 | 554 | PF00917 | 0.311 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.274 |
LIG_UBA3_1 | 4 | 8 | PF00899 | 0.454 |
LIG_WRC_WIRS_1 | 541 | 546 | PF05994 | 0.511 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.509 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.664 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.566 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.662 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.548 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.742 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.627 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.569 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.730 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.553 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.297 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.576 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.458 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.481 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.726 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.275 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.778 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.487 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.556 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.664 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.598 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.368 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.371 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.358 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.745 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.704 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.713 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.603 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.717 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.439 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.698 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.613 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.505 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.377 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.496 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.546 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.600 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.491 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.377 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.390 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.325 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.276 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.288 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.615 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.584 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.338 |
MOD_NEK2_2 | 598 | 603 | PF00069 | 0.458 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.626 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.538 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.482 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.564 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.595 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.600 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.568 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.501 |
MOD_Plk_2-3 | 570 | 576 | PF00069 | 0.538 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.444 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.344 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.401 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.499 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.778 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.456 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 428 | 433 | PF01217 | 0.568 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.431 |
TRG_NLS_MonoExtC_3 | 104 | 109 | PF00514 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHD4 | Leptomonas seymouri | 62% | 98% |
A0A0S4IWL9 | Bodo saltans | 34% | 100% |
A0A1X0P615 | Trypanosomatidae | 47% | 100% |
A0A3Q8IBF0 | Leishmania donovani | 77% | 100% |
A0A3R7MPI1 | Trypanosoma rangeli | 43% | 100% |
A4HYG8 | Leishmania infantum | 77% | 100% |
D0A0T8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AS92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QD72 | Leishmania major | 78% | 100% |
V5B132 | Trypanosoma cruzi | 44% | 100% |